Tyrosine kinase inhibitorFDA-approvedFirst-line

Brafi

Generic name: vemurafenib

How it works

Blocks the activity of the BRAF V600E mutation in melanoma cells, preventing cancer growth.

Cancer types

Melanoma— BRAF V600E mutation-positive

Efficacy

In clinical trials, around 50% of patients with BRAF V600E mutation achieved an objective response, with median progression-free survival of approximately 6 months.

Side effects

Severe

This treatment carries a higher risk of serious side effects. Close medical monitoring is required throughout treatment.

Evidence from research

StudyCancer typeStageEfficacy
Comparing Treatments for Hairy Cell LeukemiaLeukemiaphase-2—Source →
Melanoma Cells Resist Vemurafenib through Mitochondrial ChangesMelanomalab-study—Source →
New Compound May Help Fight Melanoma ResistanceMelanomalab-study—Source →
Vemurafenib May Help Fight Melanoma by Triggering Cell DeathMelanomalab-study—Source →
Researchers Identify New Way to Overcome Resistance to Cancer TreatmentMelanomalab-study—Source →
Researchers Create Melanoma Cell Lines Resistant to Cancer TreatmentMelanomalab-study—Source →
Real-world study of melanoma treatment in GermanyMelanomaobservationalMedian overall survival was 21.6 months in patients without brain metastases and 7.4 months in patients with brain metastases.Source →
Cobimetinib Plus Vemurafenib Shows Antitumor Activity in Advanced Solid TumorsMelanomaphase-2The disease control rate was 68% and the objective response rate was 57%.Source →
USP18 may help melanoma cells resist cancer treatmentMelanomalab-study—Source →
New Vemurafenib Derivatives Show Promise as Melanoma TreatmentMelanomalab-study—Source →
Switching to Atezolizumab After 3 Months May Not Help Advanced Melanoma PatientsMelanomaphase-2Median progression-free survival was 13.9 months in patients who continued vemurafenib plus cobimetinib, compared to 5.9 months in those who switched to atezolizumab.Source →
Researchers Identify Potential Target for Overcoming Melanoma ResistanceMelanomalab-study—Source →
Combination Therapy Shows Promise in Advanced Colorectal CancerColorectal Cancerphase-2The disease control rate was 52% (95% CI, 35 to 65), and the objective response rate was 30% (95% CI, 14 to 50).Source →
New way to deliver cancer drugs to melanoma cellsMelanomalab-studyBoth DAB- and VEM-loaded NMs elicited enhanced response with respect to free drug treatments in 4 different melanoma cell lines.Source →
Alternative mRNA Splicing in Melanoma Cells Resistant to VemurafenibMelanomalab-study—Source →
Vemurafenib's Side Effect Linked to Enzyme InhibitionMelanomalab-study—Source →
BRAF Inhibitor Resistance Linked to Protein PYK2 in MelanomaMelanomalab-studyIncreased expressions of p-PYK2 in melanoma patients were positively correlated with advanced stage (p = 0.002), metastasis (p < 0.001), and Clark grade (p < 0.001), and were also associated with short overall survival [hazard ratio (HR) = 3.304, p = 0.007] and progression-free survival (HR = 2.930, p = 0.001).Source →
Combining Palbociclib and Vemurafenib in Metastatic Melanoma TreatmentMelanomaphase-1/2The median progression-free survival was 2.8 months, and 5 (27.8%) patients showed a clinical response.Source →
Vemurafenib May Help Hairy Cell Leukemia Patients Before Standard TreatmentLeukemiaobservationalAfter a standard course of cladribine chemotherapy, 18 patients (90%) experienced complete clinical remission and 2 patients (10%) experienced partial remission with residual splenomegaly.Source →

This information is provided for general education only and is not medical advice. Always consult a qualified healthcare professional before making treatment decisions.